EGFR c.89-31400T>G

Variant ID: 7-55178579-T-G

NM_005228.3(EGFR):c.89-31400T>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs12668175
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Variants in human papillomavirus receptor and associated genes are associated with type-specific HPV infection and lesion progression of the cervix.

Oncotarget
Zou, Jian J; Cao, Zhu Z; Zhang, Jianyang J; Chen, Tingting T; Yang, Shizhou S; Huang, Yongjie Y; Hong, Die D; Li, Yang Y; Chen, Xiaojing X; Wang, Xinyu X; Cheng, Xiaodong X; Lu, Weiguo W; Xie, Xing X
Publication Date: 2016-06-28

Variant appearance in text: rs12668175
PubMed Link: 27223085
Variant Present in the following documents:
  • Main text
  • oncotarget-07-40135.pdf
View BVdb publication page



A two-stage case-control study of EGFR polymorphisms and breast cancer risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Hong, Young-Seoub YS; Deming, Sandra L SL; Gao, Yu-Tang YT; Long, Ji-Rong JR; Shu, Xiao-Ou XO; Cai, Qiuyin Q; Lu, Wei W; Zheng, Wei W
Publication Date: 2009-02

Variant appearance in text: rs12668175
PubMed Link: 19190167
Variant Present in the following documents:
  • Main text
View BVdb publication page